The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.

Annals of human genetics ·Vol. 32 ·No. 3 ·1969-01-00 ·Pages 261-9

Emery AE, Smith CA, Sanger R

Abstract

暂无摘要

MeSH Terms

Adolescent Adult Aged Blood Group Antigens Child Child, Preschool Color Vision Defects/genetics Creatine Kinase/blood Female Genes Humans Male Middle Aged Muscular Dystrophies/genetics Recombination, Genetic Sex Chromosomes

Chemicals

Blood Group Antigens Creatine Kinase

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Emery A E

Smith C A

Sanger R

Article Info

Journal

Annals of human genetics

Abbr.

Ann Hum Genet

ISSN

0003-4800

DOI

10.1111/j.1469-1809.1969.tb00075.x

Published

1969-01-00

Pages

261-9

Language

English

Region

England

NLM ID

0416661

Subset

External Links

PubMed source DOI: 10.1111/j.1469-1809.1969.tb00075.x View journal details

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The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.

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